Linked Data
ClinVar Variation Id:
2866076
ClinVar RCV Id:
RCV003705017
MyVariant Identifiers:
chr12:g.58158295G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764512G>C , CM000674.2:g.57764512G>C | GRCh38 |
| NC_000012.11:g.58158295G>C , CM000674.1:g.58158295G>C | GRCh37 |
| NC_000012.10:g.56444562G>C | NCBI36 |
| NG_007076.1:g.7682C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1083C>G | ENSP00000518840.1:p.Ser361= | |
| ENST00000713545.1:c.*7C>G | ENSP00000518841.1:n.*7C>G | |
| ENST00000228606.9:c.1002C>G MANE Select | ENSP00000228606.4:p.Ser334= | |
| ENST00000228606.8:c.1002C>G | ENSP00000228606.4:p.Ser334= | |
| ENST00000546567.5:c.297C>G | ENSP00000449472.1:p.Ser99= | |
| ENST00000547344.5:n.1141C>G | ||
| NM_000785.3:c.1002C>G | NP_000776.1:p.Ser334= | |
| NM_000785.4:c.1002C>G MANE Select | NP_000776.1:p.Ser334= |